Intestinal Monocyte-Derived Macrophages Control Commensal-Specific Th17 Responses. Academic Article uri icon

Overview

MeSH

  • Animals
  • Antigens, CD
  • Cells, Cultured
  • Dendritic Cells
  • Integrin alpha Chains
  • Mice
  • Receptors, Chemokine

MeSH Major

  • Intestinal Mucosa
  • Macrophages
  • Microbiota
  • Th17 Cells

abstract

  • Generation of different CD4 T cell responses to commensal and pathogenic bacteria is crucial for maintaining a healthy gut environment, but the associated cellular mechanisms are poorly understood. Dendritic cells (DCs) and macrophages (Mfs) integrate microbial signals and direct adaptive immunity. Although the role of DCs in initiating T cell responses is well appreciated, how Mfs contribute to the generation of CD4 T cell responses to intestinal microbes is unclear. Th17 cells are critical for mucosal immune protection and at steady state are induced by commensal bacteria, such as segmented filamentous bacteria (SFB). Here, we examined the roles of mucosal DCs and Mfs in Th17 induction by SFB in vivo. We show that Mfs, and not conventional CD103(+) DCs, are essential for the generation of SFB-specific Th17 responses. Thus, Mfs drive mucosal T cell responses to certain commensal bacteria. Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.

publication date

  • August 25, 2015

has subject area

  • Animals
  • Antigens, CD
  • Cells, Cultured
  • Dendritic Cells
  • Integrin alpha Chains
  • Intestinal Mucosa
  • Macrophages
  • Mice
  • Microbiota
  • Receptors, Chemokine
  • Th17 Cells

Research

keywords

  • Journal Article

Identity

Language

  • eng

PubMed Central ID

  • PMC4567384

Digital Object Identifier (DOI)

  • 10.1016/j.celrep.2015.07.040

PubMed ID

  • 26279572

Additional Document Info

start page

  • 1314

end page

  • 1324

volume

  • 12

number

  • 8